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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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23 March 2015 |
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Main ID: |
NCT02215239 |
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Date of registration:
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11/08/2014 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Development of Workplace Physical Activity Promotion Models in Taiwan
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Scientific title:
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Development of Workplace Physical Activity Promotion Models in Taiwan |
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Date of first enrolment:
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January 2014 |
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Target sample size:
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240 |
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Recruitment status: |
Recruiting |
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URL:
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http://clinicaltrials.gov/show/NCT02215239 |
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Study type:
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Interventional |
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Study design:
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Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research
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Phase:
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N/A
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Countries of recruitment
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Taiwan
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Contacts
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Name:
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Meng-Yueh Chien |
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Address:
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Telephone:
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Email:
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Affiliation:
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National Taiwan University Hospital |
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Name:
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Meng-Yueh Chien, Doctor |
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Address:
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Telephone:
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02-33668141 |
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Email:
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mychien@ntu.edu.tw |
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Affiliation:
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Name:
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Meng-Yueh Chien, Doctor |
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Address:
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Telephone:
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+886-2-33668141 |
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Email:
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mychien@ntu.edu.tw |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion criteria:
- Workers tend to be seated or standing during work hours.
- Basic capability to read or verbal communication in Chinese.
Exclusion criteria:
- No other critical diseases or unstable cardiopulmonary disease, diabetes,
hypertension or neurological diseases.
- No pregnancy.
Age minimum:
20 Years
Age maximum:
65 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Occupational Health
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Intervention(s)
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Behavioral: Workplace intervention
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Primary Outcome(s)
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Change of health-related physical fitness from baseline to 16-week
[Time Frame: 16 weeks]
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Secondary Outcome(s)
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Change of physical activity from baseline to 16-week
[Time Frame: 16 weeks]
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Change of depression symptoms from baseline to 16-week
[Time Frame: 16 weeks]
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Change of sleep quality from baseline to 16-week
[Time Frame: 16 weeks]
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Change of stress from baseline to 16-week
[Time Frame: 16 weeks]
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Secondary ID(s)
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201310041RINA
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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